FDA recall Z-1351-2019

Product

Molift 2-Point sling bar, an accessory for Molift Mover 205. Item nos. 1430016 1430017 1430021

Reason for recall

The firm has received 7 reports of malfunction for the device in which the hooks have broken off, potentially leading the sling to slip out of the sling bar and causing the patient to fall.

Distribution

Domestic distribution to Arizona, Delaware, Florida, Georgia, Massachusetts, Ohio, South Carolina, Texas, Washington, and Wisconsin. Foreign distribution to Canada, Asia, Europe, and Australia.

Key facts

Status

Ongoing

Initiation date

2019-02-04

Report date

2019-05-22

Voluntary/Mandated

Voluntary: Firm initiated

Location

Gjovik, Norway

Primary source

https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-1351-2019